| Literature DB >> 31912494 |
Ester López-Gallardo1,2,3, Francisco Cammarata-Scalisi4, Sonia Emperador1,2,3, Carmen Hernández-Ainsa1,2, Mouna Habbane1,5, Ana Vela-Sebastián1, María Pilar Bayona-Bafaluy1,2,3, Julio Montoya1,2,3, Eduardo Ruiz-Pesini1,2,3,6.
Abstract
The frequency of dermatological manifestations in diseases due to mitochondrial DNA mutations is not well known, although multiple symmetric lipomatosis has been repeatedly associated to mitochondrial DNA mutations. Here, we present a patient suffering from multiple symmetric lipomatosis and other skin signs. We found a new mitochondrial DNA mutation, m.8357T>C, in the tRNALys -coding gene and, using a cybrid approach, confirmed its pathogenicity. A meta-analysis of the dermatological signs of the patient shows that they are not common in patients with confirmed mitochondrial DNA mutations and suggests that, in these cases, lipomatosis is not related to the oxidative phosphorylation dysfunction, but to an alteration of an additional function associated to particular mitochondrial tRNAs.Entities:
Keywords: dermatologic manifestations; erythema; hyperkeratosis; mitochondrial DNA mutation; multiple symmetric lipomatosis
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Year: 2020 PMID: 31912494 DOI: 10.1111/cge.13701
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438